Department of Emergency Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Emergency Medicine, University of California, Los Angeles, CA, USA.
Clin Toxicol (Phila). 2023 Mar;61(3):173-180. doi: 10.1080/15563650.2022.2159427.
Illicit opioids, consisting largely of fentanyl, novel synthetic opioids, and adulterants, are the primary cause of drug overdose fatality in the United States. Xylazine, an alpha-2 adrenergic agonist and veterinary tranquilizer, is being increasingly detected among decedents following illicit opioid overdose. Clinical outcomes in non-fatal overdose involving xylazine are unexplored. Therefore, among emergency department patients with illicit opioid overdose, we evaluated clinical outcome differences for patients with and without xylazine exposures.
This multicenter, prospective cohort study enrolled adult patients with opioid overdose who presented to one of nine United States emergency departments between 21 September 2020, and 17 August 2021. Patients with opioid overdose were screened and included if they tested positive for an illicit opioid (heroin, fentanyl, fentanyl analog, or novel synthetic opioid) or xylazine. Patient serum was analyzed liquid chromatography quadrupole time-of-flight mass spectroscopy to detect current illicit opioids, novel synthetic opioids, xylazine and adulterants. Overdose severity surrogate outcomes were: (a) cardiac arrest requiring cardiopulmonary resuscitation (primary); and (b) coma within 4 h of arrival (secondary).
Three hundred and twenty-one patients met inclusion criteria: 90 tested positive for xylazine and 231 were negative. The primary outcome occurred in 37 patients, and the secondary outcome occurred in 111 patients. Using multivariable regression analysis, patients positive for xylazine had significantly lower adjusted odds of cardiac arrest (adjusted OR 0.30, 95% CI 0.10-0.92) and coma (adjusted OR 0.52, 95% CI 0.29-0.94).
In this large multicenter cohort, cardiac arrest and coma in emergency department patients with illicit opioid overdose were significantly less severe in those testing positive for xylazine.
在美国,主要由芬太尼、新型合成阿片类药物和掺杂物组成的非法阿片类药物是导致药物过量死亡的主要原因。苯环己哌啶,一种α-2 肾上腺素能激动剂和兽医镇静剂,在非法阿片类药物过量的死者中越来越多地被检测到。涉及苯环己哌啶的非致命性药物过量的临床结果尚未得到探索。因此,在因非法阿片类药物过量而就诊于急诊室的患者中,我们评估了有和没有苯环己哌啶暴露的患者的临床结局差异。
这项多中心、前瞻性队列研究纳入了 2020 年 9 月 21 日至 2021 年 8 月 17 日期间在美国 9 家急诊室就诊的因阿片类药物过量的成年患者。如果患者的阿片类药物检测呈阳性(海洛因、芬太尼、芬太尼类似物或新型合成阿片类药物)或苯环己哌啶检测呈阳性,则对其进行筛选并纳入。患者的血清通过液相色谱-四极杆飞行时间质谱分析,以检测当前的非法阿片类药物、新型合成阿片类药物、苯环己哌啶和掺杂物。替代药物过量严重程度的结果为:(a)需要心肺复苏的心脏骤停(主要结果);和(b)到达后 4 小时内昏迷(次要结果)。
321 名患者符合纳入标准:90 名患者检测出苯环己哌啶阳性,231 名患者检测出苯环己哌啶阴性。37 名患者发生主要结局,111 名患者发生次要结局。使用多变量回归分析,苯环己哌啶检测阳性的患者心脏骤停(调整后的比值比 0.30,95%置信区间 0.10-0.92)和昏迷(调整后的比值比 0.52,95%置信区间 0.29-0.94)的调整后 odds 显著降低。
在这项大型多中心队列研究中,急诊室因非法阿片类药物过量的患者中,苯环己哌啶检测阳性的患者的心脏骤停和昏迷程度明显较轻。